A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17599137



Internal ID21791182
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:25209368..25209368hg38UCSC Ensembl
chr12:25362302..25362302hg19UCSC Ensembl
Cytoband12p12.1
Allele length
AssemblyAllele length
hg38204
hg19204
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6096287
Supporting Variants
Samples
Known GenesKRAS
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17599137
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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